These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

280 related articles for article (PubMed ID: 1632438)

  • 1. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: a new autosomal recessive syndrome.
    Richieri-Costa A; Pereira SC
    Am J Med Genet; 1992 Mar; 42(5):681-7. PubMed ID: 1632438
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfeet in male patients.
    Richieri-Costa A; Pereira SC
    Am J Med Genet; 1993 Oct; 47(5):707-9. PubMed ID: 8267000
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The Richieri-Costa and Pereira form of acrofacial dysostosis: first case in a non-Brazilian infant.
    Walter-Nicolet E; Coëslier A; Joriot S; Kacet N; Moerman A; Manouvrier-Hanu S
    Am J Med Genet; 1999 Dec; 87(5):430-3. PubMed ID: 10594883
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: another affected Brazilian patient born to consanguineous parents.
    Richieri-Costa A; Brandão-Almeida IL
    Am J Med Genet; 1997 Aug; 71(2):233-5. PubMed ID: 9217230
    [No Abstract]   [Full Text] [Related]  

  • 5. Aarskog syndrome in a Brazilian boy born to consanguineous parents.
    Guion-Almeida ML; Richieri-Costa A
    Am J Med Genet; 1992 Jul; 43(5):808-10. PubMed ID: 1642267
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal recessive Robinow-like syndrome with anterior chamber cleavage anomalies.
    Saal HM; Greenstein RM; Weinbaum PJ; Poole AE
    Am J Med Genet; 1988 Jul; 30(3):709-18. PubMed ID: 3189394
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Probable Marden-Walker syndrome: evidence for autosomal recessive inheritance.
    Temtamy SA; Shoukry AS; Raafat M; Mihareb S
    Birth Defects Orig Artic Ser; 1975; 11(2):104-8. PubMed ID: 1227520
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome.
    Richieri-Costa A; Colletto GM; Gollop TR; Masiero D
    Am J Med Genet; 1985 Apr; 20(4):631-8. PubMed ID: 2986457
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Further evidence for genetic heterogeneity of whistling face or Freeman-Sheldon syndrome in a Chinese family.
    Wang TR; Lin SJ
    Am J Med Genet; 1987 Oct; 28(2):471-5. PubMed ID: 3425620
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Auditory canal atresia, humeroscapular synostosis, and other skeletal abnormalities: confirmation of the autosomal recessive "SAMS" syndrome.
    ter Heide H; Bulstra SK; Reekers A; Schrander JJ; Schrander-Stumpel CT
    Am J Med Genet; 2002 Jul; 110(4):359-64. PubMed ID: 12116210
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Total anonychia congenita and microcephaly with normal intelligence: a new autosomal-recessive syndrome?
    Teebi AS; Kaurah P
    Am J Med Genet; 1996 Dec; 66(3):257-60. PubMed ID: 8985482
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies.
    Malpuech G; Demeocq F; Palcoux JB; Vanlieferinghen P
    Am J Med Genet; 1983 Dec; 16(4):475-80. PubMed ID: 6660246
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A familial syndrome with micrognathia, cleft palate, short neck and stature, vertebral anomalies and mental retardation.
    Mathieu M; De Broca A; Bony H; Piussan C
    Genet Couns; 1993; 4(4):299-303. PubMed ID: 8110419
    [TBL] [Abstract][Full Text] [Related]  

  • 14. EEC syndrome: report on 20 new patients, clinical and genetic considerations.
    Rodini ES; Richieri-Costa A
    Am J Med Genet; 1990 Sep; 37(1):42-53. PubMed ID: 2240042
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autosomal recessive cleft lip/palate, ectodermal dysplasia, and minor acral anomalies: report of a Brazilian family.
    Richieri-Costa A; Guion-Almeida ML; Freire-Maia N; Pinheiro M
    Am J Med Genet; 1992 Sep; 44(2):158-62. PubMed ID: 1456284
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E; Palmieri A; Bertola A; Bellini C
    Genet Couns; 1995; 6(4):309-12. PubMed ID: 8775417
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Brief clinical report: autosomal recessive anophthalmia with multiple congenital abnormalities--type Waardenburg.
    Richieri-Costa A; Gollop TR; Otto PG
    Am J Med Genet; 1983 Apr; 14(4):607-15. PubMed ID: 6846395
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A child with sclerocornea, short limbs, short stature, and distinct facial appearance.
    Thompson EM; Winter RM
    Am J Med Genet; 1988 Jul; 30(3):719-24. PubMed ID: 3055984
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family.
    Richieri-Costa A; Guion-Almeida ML; Pagnan NA
    Am J Med Genet; 1992 Dec; 44(6):800-2. PubMed ID: 1481850
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity.
    Nakata NM; Guion-Almeida ML; Richieri-Costa A
    Am J Med Genet; 1993 Sep; 47(3):330-2. PubMed ID: 8135276
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.